首页> 外文期刊>Brain research >Glutamate-stimulated release of norepinephrine in hippocampal slices of animal models of attention-deficit/hyperactivity disorder (spontaneously hypertensive rat) and depression/anxiety-like behaviours (Wistar-Kyoto rat).
【24h】

Glutamate-stimulated release of norepinephrine in hippocampal slices of animal models of attention-deficit/hyperactivity disorder (spontaneously hypertensive rat) and depression/anxiety-like behaviours (Wistar-Kyoto rat).

机译:谷氨酸刺激的注意力缺陷/多动障碍(自发性高血压大鼠)和抑郁/焦虑样行为(Wistar-Kyoto大鼠)动物模型海马片中的去甲肾上腺素释放。

获取原文
获取原文并翻译 | 示例
           

摘要

Norepinephrine is known to play an integral role in different aspects of behaviour, such as attention and arousal. It has also been implicated in the neurobiology of attention-deficit/hyperactivity disorder (ADHD). The present study was undertaken to determine the differential effects of glutamate on norepinephrine release in hippocampal slices of several rat strains. Two of the strains used in this study model behavioural disorders i.e. spontaneously hypertensive rats (SHR) mimic the behavioural characteristics of ADHD and Wistar-Kyoto (WKY) rats have been used to model depression/anxiety-like behaviours. To achieve the aims of this study, an in vitro superfusion technique was used to determine glutamate-stimulated release of radioactively labelled norepinephrine in hippocampal slices. The results show (1) SHR and Wistar rats released significantly more [(3)H]norepinephrine in response to a 1-min pulse of glutamate (1 mM) than WKY, Sprague-Dawley and Long-Evans rats. (2) Glutamate-stimulated release of [(3)H]norepinephrine was reduced by the AMPA receptor antagonist, CNQX (1 muM), suggesting that AMPA receptors are involved. (3) Exposure of hippocampal slices to a second and third 1-min pulse of glutamate revealed significant decreases in the peaks of [(3)H]norepinephrine release suggesting internalization of AMPA receptors. The rate of AMPA receptor internalization was slower in SHR than in WKY. (4) The NMDA receptor antagonist, MK-801 (10 microM) increased glutamate-stimulated release of [(3)H]norepinephrine in SHR hippocampus. This effect was blocked by CNQX, suggesting that AMPA receptors were required for the NMDA effect and that there was an NMDA component of AMPA receptor internalization in SHR hippocampus which was not evident in WKY. The present findings reveal a novel NMDA component that influences AMPA receptor-mediated regulation of norepinephrine release in SHR hippocampus.
机译:已知去甲肾上腺素在行为的不同方面(例如注意力和唤醒)起着不可或缺的作用。它也与注意力缺陷/多动障碍(ADHD)的神经生物学有关。进行本研究以确定谷氨酸对几种大鼠品系的海马切片中去甲肾上腺素释放的差异作用。本研究中使用的两种菌株可以模拟行为障碍,即模仿ADHD和Wistar-Kyoto(WKY)大鼠行为特征的自发性高血压大鼠(SHR)已用于模拟抑郁/焦虑症行为。为了实现本研究的目的,使用了体外超融合技术来确定谷氨酸刺激的海马切片中放射性标记的去甲肾上腺素的释放。结果显示(1)SHR和Wistar大鼠在响应1分钟谷氨酸(1 mM)脉冲后释放的[[3)H]去甲肾上腺素明显高于WKY,Sprague-Dawley和Long-Evans大鼠。 (2)AMPA受体拮抗剂CNQX(1μM)降低了谷氨酸刺激的[(3)H]去甲肾上腺素的释放,表明AMPA受体参与其中。 (3)将海马切片暴露于谷氨酸的第二和第三个1分钟脉冲后发现[(3)H]去甲肾上腺素释放的峰值显着降低,表明AMPA受体内在化。 SHR中AMPA受体内在化的速度比WKY中慢。 (4)NMDA受体拮抗剂MK-801(10 microM)增加了谷氨酸刺激的SHR海马体中[(3)H]去甲肾上腺素的释放。该作用被CNQX阻断,表明NMDA效应需要AMPA受体,并且SHR海马中有AMPA受体内在化的NMDA成分,这在WKY中不明显。目前的发现揭示了一种新的NMDA成分,该成分影响AMPA受体介导的SHR海马中去甲肾上腺素释放的调节。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号